Authors: SCHOLLEN E VANDENBERK P CASSIMAN JJ MATTHIJS G

Citation: E. Schollen et al., DEVELOPMENT OF REVERSE DOT-BLOT SYSTEM FOR SCREENING OF MITOCHONDRIAL-DNA MUTATIONS ASSOCIATED WITH LEBER HEREDITARY OPTIC ATROPHY, Clinical chemistry, 43(1), 1997, pp. 18-23

Authors: VANDENBERK P DESMET L FABRY G

Citation: P. Vandenberk et al., FINGER FRACTURES IN CHILDREN TREATED WITH ABSORBABLE PINS, Journal of pediatric orthopedics. Part B, 5(1), 1996, pp. 27-30

Authors: MATTHIJS G LEGIUS E SCHOLLEN E VANDENBERK P JAEKEN J BARONE R FIUMARA A VISSER G LAMBERT M CASSIMAN JJ

Citation: G. Matthijs et al., EVIDENCE FOR GENETIC-HETEROGENEITY IN THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I (CDG1), Genomics, 35(3), 1996, pp. 597-599

Authors: MATTHIJS G VANDENBERK P LEGIUS E JAEKEN J CASSIMAN JJ

Citation: G. Matthijs et al., CONFIRMATION OF LINKAGE OF CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-1 (CDG1) TO CHROMOSOME 16P13.13-P13.11 AND LINKAGE DISEQUILIBRIUM TO D16S414, D16S497 AND D16S519, Cytogenetics and cell genetics, 72(4), 1996, pp. 16-16

Authors: SMEIJSTERS H VANDENBERK P

Citation: H. Smeijsters et P. Vandenberk, MUSIC-THERAPY WITH A CLIENT SUFFERING FROM MUSICOGENIC EPILEPSY - A NATURALISTIC QUALITATIVE SINGLE-CASE RESEARCH, The Arts in psychotherapy, 22(3), 1995, pp. 249-263